A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17583609



Internal ID21775652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14326764..14327080hg38UCSC Ensembl
chr11:14348310..14348626hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6037240
Supporting Variants
Samples
Known GenesRRAS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17583609
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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